Name

abnormality of the periventricular white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the periventricular white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cerebral white matter Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral white matter phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the brainstem white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the brainstem white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar white matter Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cerebellar white matter relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

white matter of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in white matter of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Leukoencephalopathy with vanishing white matter Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with vanishing white matter phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vanishing White Matter Leukodystrophy with Ovarian Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vanishing White Matter Leukodystrophy with Ovarian Failure from the curated CTD Gene-Disease Associations dataset.

frontal-limbic white matter pathway associations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontal-limbic white matter pathway associations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral white matter hyperintensities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral white matter hyperintensities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intracranial hemorrhage; white matter disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intracranial hemorrhage; white matter disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

homocysteine metabolism, cognition, and white matter lesions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease homocysteine metabolism, cognition, and white matter lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral white matter lesions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral white matter lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

White matter integrity Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White matter integrity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White matter integrity (interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White matter integrity (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White matter microstructure (global fractional anisotropy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White matter microstructure (global fractional anisotropy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White matter hyperintensity burden Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White matter hyperintensity burden phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

hypointensity of cerebral white matter on mri Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the hypointensity of cerebral white matter on mri phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

cerebral white matter atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebral white matter atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

white matter neuronal heterotopia Gene Set

From HPO Gene-Disease Associations

genes associated with the white matter neuronal heterotopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse white matter abnormalities Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse white matter abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

focal white matter lesions Gene Set

From HPO Gene-Disease Associations

genes associated with the focal white matter lesions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse demyelination of the cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse demyelination of the cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse swelling of cerebral white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse swelling of cerebral white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

deep white matter hypodensities Gene Set

From HPO Gene-Disease Associations

genes associated with the deep white matter hypodensities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multifocal cerebral white matter abnormalities Gene Set

From HPO Gene-Disease Associations

genes associated with the multifocal cerebral white matter abnormalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe demyelination of the white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the severe demyelination of the white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy demyelination of subcortical white matter Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy demyelination of subcortical white matter phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

subcortical white matter calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the subcortical white matter calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypointensity of cerebral white matter on mri Gene Set

From HPO Gene-Disease Associations

genes associated with the hypointensity of cerebral white matter on mri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal spinal cord white matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brain white matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brain white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellum white matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellum white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

leukoencephalopathy with vanishing white matter Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with vanishing white matter phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephaly with vanishing white matter Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephaly with vanishing white matter phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral white matter Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cerebral white matter in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

periventricular gray matter heterotopia Gene Set

From HPO Gene-Disease Associations

genes associated with the periventricular gray matter heterotopia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

white mater abnormalities in the posterior periventricular region Gene Set

From HPO Gene-Disease Associations

genes associated with the white mater abnormalities in the posterior periventricular region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Particulate Matter Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Particulate Matter from the curated CTD Gene-Chemical Interactions dataset.

verbal learning, verbal memory, and regional cortical gray matter density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease verbal learning, verbal memory, and regional cortical gray matter density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

matter Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term matter in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

matters Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term matters in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

matterinduced Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term matterinduced in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Gray matter volume (schizophrenia interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Gray matter volume (schizophrenia interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

gray matter heterotopias Gene Set

From HPO Gene-Disease Associations

genes associated with the gray matter heterotopias phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal spinal cord grey matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord grey matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cerebral gray matter Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cerebral gray matter in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Superior colliculus, motor related, intermediate white layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, intermediate white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

intermediate white layer of SC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in intermediate white layer of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Superior colliculus, motor related, deep white layer Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Superior colliculus, motor related, deep white layer relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

deep white layer of SC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in deep white layer of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

White sponge nevus of cannon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the White sponge nevus of cannon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wolff-Parkinson-White Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wolff-Parkinson-White Syndrome from the curated CTD Gene-Disease Associations dataset.

wolff-parkinson-white syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease wolff-parkinson-white syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

white piedra Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease white piedra in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

wolff-parkinson-white syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease wolff-parkinson-white syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

white Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term white in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

CIDEC_KO_GDS3776_552_mouse_Brown and white adipose tissues Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the CIDEC_KO_GDS3776_552_mouse_Brown and white adipose tissues gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

PRDM16_DEPLETION_GDS4021_460_mouse_WAT - white adipose tissue (stromal-vascular cells) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the PRDM16_DEPLETION_GDS4021_460_mouse_WAT - white adipose tissue (stromal-vascular cells) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

SFRP5_KO_GDS4988_27_mouse_gonadal white adipose tissue HFD Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the SFRP5_KO_GDS4988_27_mouse_gonadal white adipose tissue HFD gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

white fat cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the white fat cell differentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of white fat cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of white fat cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of white fat cell proliferation biological process from the curated GO Biological Process Annotations dataset.

White blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White blood cell types Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White blood cell types phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

C-reactive protein and white blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the C-reactive protein and white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

white forelock Gene Set

From HPO Gene-Disease Associations

genes associated with the white forelock phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

white eyelashes Gene Set

From HPO Gene-Disease Associations

genes associated with the white eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

white eyebrow Gene Set

From HPO Gene-Disease Associations

genes associated with the white eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

wolff-parkinson-white syndrome Gene Set

From HPO Gene-Disease Associations

genes associated with the wolff-parkinson-white syndrome phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

white hair Gene Set

From HPO Gene-Disease Associations

genes associated with the white hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Wolff-Parkinson-White Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Wolff-Parkinson-White Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Suppressor of white apricot N-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Suppressor of white apricot N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased white fat cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased white adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

white spotting Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the white spotting phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased spleen white pulp amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased spleen white pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white fat cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white fat cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white fat cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spleen white pulp morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spleen white pulp morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased white fat cell size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intermingled spleen red and white pulp Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intermingled spleen red and white pulp phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased spleen white pulp amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased spleen white pulp amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased white fat cell lipid droplet size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white adipose tissue physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent spleen white pulp Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent spleen white pulp phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white fat cell lipid droplet size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white adipose tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white adipose tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white fat cell size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased white fat cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white fat cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal white fat cell differentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal white fat cell differentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased white fat cell lipid droplet size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased white adipose tissue amount Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased white adipose tissue amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased white fat cell size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased white fat cell size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

[white blood cell count qtl] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [white blood cell count qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.

wolff-parkinson-white syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the wolff-parkinson-white syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

white sponge nevus 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the white sponge nevus 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

white sponge nevus 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the white sponge nevus 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

Transcriptional regulation of white adipocyte differentiation Gene Set

From Reactome Pathways

proteins participating in the Transcriptional regulation of white adipocyte differentiation pathway from the Reactome Pathways dataset.

white adipose tissue Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue white adipose tissue from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

white adipose tissue Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue white adipose tissue in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

egg white Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue egg white in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

white prepupa Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue white prepupa in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

periventricular stratum of isBL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of isBL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of SeStr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of SeStr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Periventricular region Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Periventricular region relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r3Co Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r3Co relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral septal nucleus, intermediate part, periventricular Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral septal nucleus, intermediate part, periventricular relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r6BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r6BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

dorsal peduncular cortex, periventricular part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in dorsal peduncular cortex, periventricular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r4Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r4Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of SC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of SC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of AOB Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of AOB relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of JcPV Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of JcPV relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of JcPL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of JcPL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r6Co Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r6Co relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of isBI Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of isBI relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r3Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r3Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of AStr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of AStr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of DTTh Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of DTTh relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of APal Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of APal relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r1BL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r1BL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r1BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r1BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r3Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r3Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of Ist Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of Ist relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r10BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r10BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r8Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r8Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r4Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r4Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of p1B Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of p1B relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r2Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r2Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anteroventral periventricular preoptic nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anteroventral periventricular preoptic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of PalSe Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of PalSe relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of PcPV Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of PcPV relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of PcPL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of PcPL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of OB Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of OB relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of isLim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of isLim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Periventricular zone Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Periventricular zone relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of CoPV Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of CoPV relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r7Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r7Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of p1Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of p1Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of p3ZL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of p3ZL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of Hb Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of Hb relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of PO2 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of PO2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of PO1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of PO1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r1Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r1Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Periventricular hypothalamic nucleus, posterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Periventricular hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r8BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r8BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r8Tr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r8Tr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r2BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r2BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of RtC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of RtC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m1Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m1Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of IC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of IC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of TTe Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of TTe relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of CbH Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of CbH relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r2Co Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r2Co relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m2AD Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m2AD relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m2AL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m2AL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m1AD Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m1AD relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m1AL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m1AL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of Dg Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of Dg relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r10Tr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r10Tr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r7Tr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r7Tr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of the PBC Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of the PBC relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r6Tr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r6Tr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of SeDg Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of SeDg relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r7BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r7BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r9BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r9BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r5Tr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r5Tr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r9Tr Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r9Tr relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of TPaA Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of TPaA relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular mantle of isBM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular mantle of isBM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m1B Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m1B relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of TG Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of TG relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r6Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r6Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m2ADL Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m2ADL relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r9Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r9Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r5Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r5Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r7Co Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r7Co relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r9Ve Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r9Ve relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r1Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r1Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of VTTh Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of VTTh relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of PPaA Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of PPaA relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of ITTh Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of ITTh relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of the VAP Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of the VAP relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r4Co Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r4Co relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of RMa Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of RMa relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of Pal Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of Pal relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r5BM Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r5BM relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of Str Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of Str relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r2Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r2Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r5Co Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r5Co relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anteroventral periventricular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anteroventral periventricular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of r10Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of r10Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of m2Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of m2Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of p2Lim Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of p2Lim relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular part of StrSe Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular part of StrSe relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular nucleus, preoptic portion Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular nucleus, preoptic portion relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Periventricular nodular heterotopia 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Periventricular nodular heterotopia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heterotopia, periventricular, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Heterotopia, periventricular, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked periventricular heterotopia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked periventricular heterotopia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heterotopia, periventricular, Ehlers-Danlos variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Heterotopia, periventricular, Ehlers-Danlos variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heterotopia, Periventricular, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, Ehlers-Danlos Variant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, Ehlers-Danlos Variant from the curated CTD Gene-Disease Associations dataset.

Periventricular Nodular Heterotopia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Periventricular Nodular Heterotopia from the curated CTD Gene-Disease Associations dataset.

HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HETEROTOPIA, PERIVENTRICULAR, X-LINKED DOMINANT from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, associated with Chromosome 5p Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, associated with Chromosome 5p Anomalies from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, Associated With Chromosome 5q Deletion Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, Associated With Chromosome 5q Deletion from the curated CTD Gene-Disease Associations dataset.

periventricular nodular heterotopia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease periventricular nodular heterotopia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

periventricular leukomalacia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease periventricular leukomalacia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

leukomalacia, periventricular; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukomalacia, periventricular; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; leukomalacia, periventricular; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; leukomalacia, periventricular; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; cerebral palsy; infant, premature, diseases; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; infection of amniotic sac and membranes; leukomalacia, periventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; infection of amniotic sac and membranes; leukomalacia, periventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

periventricular Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term periventricular in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

intracerebral periventricular calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the intracerebral periventricular calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

periventricular cysts Gene Set

From HPO Gene-Disease Associations

genes associated with the periventricular cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

periventricular leukomalacia Gene Set

From HPO Gene-Disease Associations

genes associated with the periventricular leukomalacia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Leukomalacia, Periventricular Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Leukomalacia, Periventricular phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

?periventricular nodular heterotopia 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?periventricular nodular heterotopia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

periventricular nodular heterotopia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the periventricular nodular heterotopia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

periventricular nodular heterotopia 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the periventricular nodular heterotopia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

periventricular heterotopia with microcephaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the periventricular heterotopia with microcephaly phenotype from the curated OMIM Gene-Disease Associations dataset.

heterotopia, periventricular, ed variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the heterotopia, periventricular, ed variant phenotype from the curated OMIM Gene-Disease Associations dataset.

heterotopia, periventricular Gene Set

From OMIM Gene-Disease Associations

genes associated with the heterotopia, periventricular phenotype from the curated OMIM Gene-Disease Associations dataset.

periventricular nucleus of hypothalamus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue periventricular nucleus of hypothalamus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

posterior periventricular nucleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue posterior periventricular nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Hypertelorism with esophageal abnormality and hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertelorism with esophageal abnormality and hypospadias from the curated CTD Gene-Disease Associations dataset.

congenital nervous system abnormality Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital nervous system abnormality Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

abnormality of glucagon secretion Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease abnormality of glucagon secretion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

gastrin secretion abnormality Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease gastrin secretion abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

brain neoplasms; chromosome aberrations; chromosome abnormality; glioma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; chromosome aberrations; chromosome abnormality; glioma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms, germ cell and embryonal; neoplasms, testis; testicular neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; dystonic disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; conjunctivitis; peripheral nervous system diseases; precancerous conditions; skin diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cleft lip; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; infertility, male; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; infertility, male; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leiomyoma; radiation injuries; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid; myeloid leukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; leukemia, myeloid, acute; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; chromosome aberrations; chromosome abnormality; dna damage; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma; carcinoma, papillary; chromosome aberrations; chromosome abnormality; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cadasil; chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cadasil; chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

torsion abnormality; vascular malformations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease torsion abnormality; vascular malformations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hyperkeratosis, epidermolytic; precancerous conditions; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chronic lymphocytic leukemia; leukemia, lymphocytic, chronic, b-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; lymphocytosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; lymphocytosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; hamartoma; hypothalamic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; dna damage; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; dna damage; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; chromosome deletion; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneuploidy; chromosome aberrations; chromosome abnormality; trisomy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneuploidy; chromosome aberrations; chromosome abnormality; trisomy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; micronuclei, chromosome-defective; radiation injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; craniosynostoses; craniosynostosis; genetic diseases, inborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

smooth pursuit eye movement abnormality Gene Set

From GAD Gene-Disease Associations

genes associated with the disease smooth pursuit eye movement abnormality in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormality Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term abnormality in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

abnormality of vitamin metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of movement Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the endometrium Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the endometrium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of thyroid morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of thyroid morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of forearm bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of forearm bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the integument Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the integument phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin d metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin d metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of myeloid leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of myeloid leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebral subcortex Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral subcortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of divalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of divalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

inflammatory abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the inflammatory abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the stomach Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the stomach phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of central motor function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of central motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vasculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of glycolipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of glycolipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of connective tissue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of connective tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of upper limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of upper limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the aortic valve Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the aortic valve phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cellular immune system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cellular immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

hearing abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the hearing abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of immune serum protein physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of immune serum protein physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of leukocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of leukocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of oral mucosa Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of oral mucosa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the urethra Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the urethra phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of brain morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of brain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the endocrine system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the endocrine system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cerebral artery Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cerebral artery phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the breast Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the breast phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the autonomic nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the autonomic nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pharynx Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

eeg abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the eeg abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femur Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femur phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the immune system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the immune system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

morphological abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin a metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin a metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the calf Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the calf phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of potassium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of potassium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the carotid arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the carotid arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of retinal arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of retinal arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the kidney Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the kidney phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circle of willis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circle of willis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hand Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hand phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pituitary gland Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pituitary gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the myocardium Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the myocardium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the biliary system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the biliary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cell cycle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cell cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of von willebrand factor Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of von willebrand factor phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of finger Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lower limb Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lower limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of long bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of long bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of thrombocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of thrombocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of neutrophils Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of neutrophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hip bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hip bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the upper urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the iris Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the iris phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lower urinary tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lower urinary tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac ventricle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cardiac ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of thyroid physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of thyroid physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of hair pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

mesangial abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the mesangial abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin b metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin b metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating fibrinogen Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating fibrinogen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the adrenal glands Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the adrenal glands phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the intestine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the respiratory system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the respiratory system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of phalanx of finger Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the musculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the musculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the duodenum Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the duodenum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skull base Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skull base phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the astrocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the astrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the urinary system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the urinary system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of basophils Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of basophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nervous system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the face Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the face phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the male genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the male genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of facial skeleton Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the posterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gingiva Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the gingiva phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the large intestine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the large intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lung Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lung phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating hormone level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating hormone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the placenta Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the placenta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ankles Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ankles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femoral neck Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the heart valves Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the heart valves phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

morphological abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of aromatic amino acid family metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of aromatic amino acid family metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of prenatal development or birth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of prenatal development or birth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of eye movement Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of eye movement phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the upper limb Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper limb phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebral vasculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ovary Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ovary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the prostate Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the prostate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of digit Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of digit phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limbs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limbs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the testis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the testis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the anterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dental eruption Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of dental eruption phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the clavicle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the clavicle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of homocysteine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of homocysteine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the knees Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the knees phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the coronary arteries Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the coronary arteries phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cardiovascular system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cardiovascular system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin adnexa Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin adnexa phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pleura Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pleura phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hair Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of interleukin secretion Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of interleukin secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood and blood-forming tissues Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of transition element cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of transition element cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of tryptophan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of tryptophan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the head Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of head or neck Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of head or neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the mandible Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the mandible phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional respiratory abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional respiratory abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of humoral immunity Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of humoral immunity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

neurodevelopmental abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the neurodevelopmental abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of taste sensation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of taste sensation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of renin-angiotensin system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of renin-angiotensin system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of pancreas physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of pancreas physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skeletal system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skeletal system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of primary teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of primary teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the thorax Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the thorax phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the thyroid gland Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the thyroid gland phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the abdomen Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the abdomen phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebrum Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebrum phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebrospinal fluid Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebrospinal fluid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the menstrual cycle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the menstrual cycle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

behavioral abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the behavioral abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the oral cavity Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the oral cavity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cholesterol metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cholesterol metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of granulocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of granulocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of monovalent inorganic cation homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of monovalent inorganic cation homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the fundus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the fundus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of forebrain morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of forebrain morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the tongue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the tongue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of acid-base homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of acid-base homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vertebrae Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vertebrae phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the spinal cord Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

vascular skin abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the vascular skin abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of iron homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of iron homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of refraction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of refraction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood volume homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dna repair Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of dna repair phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nose Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nose phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nitrogen compound homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nitrogen compound homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of central nervous system electrophysiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of central nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nervous system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of erythrocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of erythrocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of liposaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of liposaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femoral neck or head region Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the urinary system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the urinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vasculature of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vasculature of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the glomerulus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the glomerulus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of unsaturated fatty acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of unsaturated fatty acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiac morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cardiac morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating protein level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating protein level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of copper homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of copper homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

prenatal maternal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the prenatal maternal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the humeral diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the humeral diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

phenotypic abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the phenotypic abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of reproductive system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the uterus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the uterus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of female internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of female internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the curvature of the cornea Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the curvature of the cornea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the metaphyses Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the metaphyses phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

functional abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the functional abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gastrointestinal tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the gastrointestinal tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the common coagulation pathway Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the common coagulation pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of male internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the hypothalamus-pituitary axis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the hypothalamus-pituitary axis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of fatty-acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of fatty-acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the genitourinary system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the genitourinary system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cytokine secretion Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cytokine secretion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

growth abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the growth abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the choroid Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the choroid phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the globe Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the globe phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of radial diaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of radial diaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of sodium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of sodium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of muscle morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of muscle morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear ossicles Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear ossicles phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cells of the monocyte/macrophage lineage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cells of the monocyte/macrophage lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lower limb joint Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the uvea Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the uvea phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

biliary tract abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the biliary tract abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the abdominal organs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the abdominal organs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the esophagus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the esophagus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the retina Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the retina phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the penis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the penis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood circulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the radius Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the radius phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of urine homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of urine homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the costochondral junction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cerebral cortex Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cerebral cortex phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

venous abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the venous abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of extrapyramidal motor function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of extrapyramidal motor function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone marrow cell morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone marrow cell morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the liver Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the liver phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of proteoglycan metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of proteoglycan metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of fluid regulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of fluid regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of upper limb metaphysis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of upper limb metaphysis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pylorus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pylorus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of adipose tissue Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of adipose tissue phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the anterior pituitary Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nasopharynx Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nasopharynx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the intervertebral disk Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the intervertebral disk phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the stapes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the stapes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the gallbladder Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the gallbladder phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the coagulation cascade Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the coagulation cascade phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the left ventricle Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the left ventricle phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of zinc homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of pelvic girdle bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of pelvic girdle bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

generalized abnormality of skin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the generalized abnormality of skin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lower limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lower limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lipid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of b cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of b cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the left ventricular outflow tract Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the left ventricular outflow tract phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of carbohydrate metabolism/homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of muscle physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of muscle physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the glial cells Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the glial cells phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of dental structure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of dental structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the upper arm Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the upper arm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ulna Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ulna phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the femoral head Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of corneal endothelium Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of corneal endothelium phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of lymphocytes Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of lymphocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of corneal thickness Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of corneal thickness phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the mouth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the mouth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the vitamin b12 metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vitamin b12 metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limb bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of magnesium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of magnesium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the small intestine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the genital system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the genital system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the aorta Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the aorta phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the female genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the female genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the humerus Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the humerus phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cardiovascular system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cardiovascular system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

morphological abnormality of the central nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the morphological abnormality of the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of complement system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of complement system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cells of the erythroid lineage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cells of the erythroid lineage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

chorioretinal abnormality Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the chorioretinal abnormality phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of sulfur amino acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of sulfur amino acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating cortisol level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating cortisol level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of prothrombin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of prothrombin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the curvature of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of coagulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of coagulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the cervical spine Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the cervical spine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the skull Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the skull phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of carboxylic acid metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of carboxylic acid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the middle ear Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the middle ear phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the pancreas Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the pancreas phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skeletal morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skeletal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the lens Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the lens phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of b cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of b cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of body weight Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of body weight phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of temperature regulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of temperature regulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the systemic arterial tree Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the systemic arterial tree phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the rib cage Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the rib cage phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of glycoprotein metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of glycoprotein metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of vitamin e metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of vitamin e metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of cell physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of cell physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the retinal vasculature Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the retinal vasculature phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of skin pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of skin pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of ion homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of ion homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nervous system Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of macrophages Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of macrophages phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of calcium homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of calcium homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of male external genitalia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of male external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of body height Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of body height phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of polysaccharide metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of polysaccharide metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the intrinsic pathway Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the intrinsic pathway phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of eosinophils Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of eosinophils phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the macula Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the macula phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of epidermal morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of epidermal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of higher mental function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of higher mental function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of limb bone Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of limb bone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the ribs Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the ribs phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of nucleobase metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of nucleobase metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the forearm Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the forearm phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of purine metabolism Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of purine metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of serum cytokine level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of serum cytokine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of immune system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of immune system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating leptin level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating leptin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the nephron Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the nephron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of circulating glucocorticoid level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of circulating glucocorticoid level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the level of lipoprotein cholesterol Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the neck Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the falx cerebri Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the falx cerebri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of myeloid leukocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of myeloid leukocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of gastrointestinal vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of gastrointestinal vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the extraocular muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the extraocular muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the choanae Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the choanae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycolipid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glycolipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasal cavity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasal cavity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the immune system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the immune system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of reticulocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of reticulocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper lip Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cochlea Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cochlea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of von willebrand factor Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of von willebrand factor phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cardiac ventricle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cardiac ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the intestine Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the gingiva Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the gingiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lung Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lung phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the gastrointestinal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the gastrointestinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the basal ganglia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vena cava Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vena cava phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of sharpey fibers Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of sharpey fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thorax Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the hypothalamus-pituitary axis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the hypothalamus-pituitary axis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the head Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cornea Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the frontal sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the frontal sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of metacarpophalangeal joint Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the femoral neck or head region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the intrahepatic bile duct Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the intrahepatic bile duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of fluid regulation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of fluid regulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the philtrum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the philtrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the dentate nucleus Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fallopian tube Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the fallopian tube phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of secondary sexual hair Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pineal gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pineal gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the crus of the helix Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the acetabulum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the acetabulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of vision Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sense of smell Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sense of smell phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of central somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of central somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of permanent molar morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of permanent molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lower limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lower limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of muscle physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of muscle physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the parathyroid physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the parathyroid physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the corpus callosum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the corpus callosum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the achilles tendon Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the achilles tendon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the myocardium Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the myocardium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of complement system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of complement system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the medullary cavity of the long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the medullary cavity of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the phalanges of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycoprotein metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glycoprotein metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of blood glucose concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the renal tubule Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the renal tubule phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the shoulder Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the shoulder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the 3rd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 3rd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of chromosome condensation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of chromosome condensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of prostaglandin metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of prostaglandin metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neurodevelopmental abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the neurodevelopmental abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of connective tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of connective tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of thumb phalanx Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of thumb phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the odontoid process Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the odontoid process phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of alanine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of alanine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atlantoaxial abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the atlantoaxial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lower limb Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lower limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of thrombocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of thrombocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the posterior pituitary Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thymus Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the thymus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vestibulocochlear nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vestibulocochlear nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of prenatal development or birth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of prenatal development or birth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper limb Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the upper limb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of binocular vision Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of binocular vision phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasal septum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cation homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cation homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thyroid gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the thyroid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the bladder Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the alveolar ridges Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of forebrain morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of forebrain morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cerebral artery Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cerebral artery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the choroid plexus Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the choroid plexus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of circulating protein level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of circulating protein level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of pancreas morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pancreas morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the seventh cranial nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the seventh cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the labia minora Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the labia minora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the palmar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

biliary tract abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the biliary tract abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cells of the lymphoid lineage Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cells of the lymphoid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the aortic arch Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb epiphysis morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized abnormality of skin Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized abnormality of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of b cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of b cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cardiac morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cardiac morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the glial cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the glial cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the aryepiglottic fold Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the aryepiglottic fold phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cells of the erythroid lineage Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cells of the erythroid lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of prothrombin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of prothrombin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the phalanges of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of b cell physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of b cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature of the limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the subungual region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the subungual region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of thyroid morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of thyroid morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the scalp Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the scalp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inflammatory abnormality of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the inflammatory abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the frontal hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the frontal hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the renal collecting system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the renal collecting system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pulmonary vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pulmonary vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the middle phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the middle phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the femoral metaphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of oral mucosa Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of peripheral nerves Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of peripheral nerves phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the acoustic reflex Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the acoustic reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the middle ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the middle ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of potassium homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of potassium homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lip Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pituitary gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tubulointerstitial abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the tubulointerstitial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the dental pulp Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the dental pulp phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cysteine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cysteine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the thenar eminence Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of ganglioside metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of ganglioside metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the middle phalanges of the toes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the middle phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of humoral immunity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of humoral immunity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sixth cranial nerve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sixth cranial nerve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of calvarial morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of calvarial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the hip joint Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the humeral metaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the humeral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of urine bicarbonate concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of urine bicarbonate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the genitourinary system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the genitourinary system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lymphatic vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lymphatic vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fascia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the fascia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ear Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the radius Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the liver Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the liver phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb metaphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of dental color Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of dental color phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of alkaline phosphatase activity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of alkaline phosphatase activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal phalanges of the hand Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the larynx Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the larynx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

chorioretinal abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the chorioretinal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of circulating hormone level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of circulating hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the salivary glands Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the salivary glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cell physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of primary molar morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of primary molar morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of copper homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of copper homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sacroiliac joint Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the diaphragm Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of movement Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lacrimal duct Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lacrimal duct phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal tibial epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the aortic valve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the aortic valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the corticospinal tract Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the corticospinal tract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the endocrine system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the endocrine system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the tarsal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the tarsal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the soft palate Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the soft palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the adrenal glands Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the adrenal glands phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the periorbital region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the periorbital region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the respiratory system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the respiratory system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of fontanelles Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the septum pellucidum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the septum pellucidum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of renal excretion Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of renal excretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the premaxilla Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the premaxilla phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

eeg abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the eeg abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of renin-angiotensin system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of renin-angiotensin system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of pancreas physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pancreas physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

c1-c2 vertebral abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the c1-c2 vertebral abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the skin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lower lip Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lower lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pectoral muscle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pectoral muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of descemet's membrane Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of descemet's membrane phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sclera Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sclera phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

phenotypic abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the phenotypic abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of circulating adrenocorticotropin level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of circulating adrenocorticotropin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the radial head Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the radial head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of saccadic eye movements Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasolabial region Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasolabial region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of somatosensory evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of somatosensory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the uvea Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the uvea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of female external genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of female external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of tyrosine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of tyrosine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of extrapyramidal motor function Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of extrapyramidal motor function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature of the thorax Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the thorax phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cardiovascular system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cardiovascular system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the proximal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the rectum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the rectum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphysis of the middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of carbohydrate metabolism/homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of carbohydrate metabolism/homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ulna Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the supraorbital ridges Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the supraorbital ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the coagulation cascade Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the coagulation cascade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycosaminoglycan metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glycosaminoglycan metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the extrinsic pathway Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the extrinsic pathway phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skeletal morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skeletal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

morphological abnormality of the vestibule of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the morphological abnormality of the vestibule of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skin adnexa Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skin adnexa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of limb bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of limb bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the mitral valve Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the mitral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of orotic acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of orotic acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of neutrophil physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of neutrophil physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glycine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of globe location Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of globe location phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the scapula Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the scapula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of t cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of t cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of dicarboxylic acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of dicarboxylic acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cells of the granulocytic lineage Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cells of the granulocytic lineage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the femur Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of upper limb joint Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of upper limb joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pancreatic islet cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pancreatic islet cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of long bone morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of long bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the lymphatic system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the lymphatic system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mesangial abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the mesangial abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the epiphyses of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the patella Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the patella phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

blood group antigen abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of glycolysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of glycolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the optic disc Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the optic disc phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of dermal melanosomes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of dermal melanosomes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of leucine metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of leucine metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of b cell number Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of b cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the renal cortex Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the renal cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the ventricular septum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the ventricular septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature of the pelvis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the pelvis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the fetal cardiovascular system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the fetal cardiovascular system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of nitrogen compound homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of nitrogen compound homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the palate Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the posterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the posterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the mandible Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the sinuses Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the sinuses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the pubic hair Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of proteoglycan metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of proteoglycan metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

muscle abnormality related to mitochondrial dysfunction Gene Set

From HPO Gene-Disease Associations

genes associated with the muscle abnormality related to mitochondrial dysfunction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the macula Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the macula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the styloid process of ulna Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the styloid process of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of skull ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of skull ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the musculature of the upper arm Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of vision evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of vision evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the labia majora Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the labia majora phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the genital system Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the genital system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the humerus Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the humerus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lens shape Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lens shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the uvula Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the uvula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of lateral ventricle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of lateral ventricle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of chromosome segregation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of chromosome segregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of higher mental function Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of higher mental function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

inflammatory abnormality of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the inflammatory abnormality of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of vitamin k metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of vitamin k metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the nasal bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the nasal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the conjunctiva Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the conjunctiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the chin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the chin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of cardiac atrium Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of cardiac atrium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of pain sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pain sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the distal femoral epiphysis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the menstrual cycle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the menstrual cycle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the plantar skin of foot Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the plantar skin of foot phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of pyruvate family amino acid metabolism Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of pyruvate family amino acid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sacrococcygeal pilonidal abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the sacrococcygeal pilonidal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of adrenal morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of adrenal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of carpal bone ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of carpal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of male internal genitalia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of male internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the eyelashes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cerebral vasculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cerebral vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of urine hormone level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of urine hormone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of mast cells Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of mast cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of globe size Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of globe size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the eyebrow Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vascular skin abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the vascular skin abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of central nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of central nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the foramen magnum Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the foramen magnum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the phalanges of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the inner ear Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the inner ear phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of hand joint mobility Gene Set